Class IIOngoingZ-0926-2026
AVID Medical, Inc. recalls Halyard
Potential for incomplete seal on header bag.
AVID Medical, Inc.VADec 24, 2025
2025 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 73–84 of 2,908 recalls
Class IIOngoingZ-0925-2026
Zimmer Surgical Inc recalls Zimmer Dermatome AN
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025
Class IIOngoingZ-0924-2026
Zimmer Surgical Inc recalls Zimmer Air Dermatome
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025
Class IIOngoingZ-0922-2026
Medline Industries, LP recalls FORCEP
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Medline Industries, LPILDec 24, 2025
Class IIOngoingZ-0921-2026
Medline Industries, LP recalls SCISSORS
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Medline Industries, LPILDec 24, 2025
Class IIOngoingZ-0920-2026
Mindray DS USA, Inc. Dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS)
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Mindray DS USA, Inc. d…NJDec 24, 2025
Class IOngoingZ-0915-2026
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replacea…
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
GE Medical Systems Chi…Dec 24, 2025
Class IOngoingZ-0914-2026
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
GE Medical Systems Chi…Dec 24, 2025
Class IOngoingZ-0913-2026
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
GE Medical Systems Chi…Dec 24, 2025
Class IOngoingZ-0885-2026
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS)
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
Fresenius Kabi USA, LL…MADec 24, 2025
Class IIOngoingZ-0919-2026
Stryker Medical Division Of Stryker Corporation recalls Stryker Arise 1000EX mattress
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…
- Alternating Pressure Air Flotation Mattress
- Release of Material/Component prior to receiving test results
Stryker Medical Divisi…MIDec 17, 2025
Class IIOngoingZ-0918-2026
Stryker Medical Division Of Stryker Corporation recalls Stryker MV3 bariatric bed
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together.…
Stryker Medical Divisi…MIDec 17, 2025